ClinVar Miner

Submissions for variant NM_005477.3(HCN4):c.1738-6C>T

gnomAD frequency: 0.00014  dbSNP: rs760763085
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000863258 SCV000715466 likely benign not provided 2019-08-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001086547 SCV001003888 likely benign Brugada syndrome 8 2024-11-26 criteria provided, single submitter clinical testing
Athena Diagnostics RCV000863258 SCV001144126 benign not provided 2018-12-31 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV000611970 SCV001920208 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000863258 SCV001972180 likely benign not provided no assertion criteria provided clinical testing

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